Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?

Detalhes bibliográficos
Autor(a) principal: Leite, Heitor Pons [UNIFESP]
Data de Publicação: 2016
Outros Autores: Peixoto de Lima, Lucio Flavio [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
dARK ID: ark:/48912/001300000b702
Texto Completo: http://dx.doi.org/10.21037/jtd.2016.05.37
https://repositorio.unifesp.br/handle/11600/57604
Resumo: Despite the advances made in monitoring and treatment of sepsis and septic shock, many septic patients ultimately develop multiple organ dysfunction (MODS) and die, suggesting that other players are involved in the pathophysiology of this syndrome. Mitochondrial dysfunction occurs early in sepsis and has a central role in MODS development. MODS severity and recovery of mitochondrial function have been associated with survival. In recent clinical and experimental investigations, mitochondrion-target therapy for sepsis and septic shock has been suggested to reduce MODS severity and mortality. This intervention, which might be named "metabolic resuscitation", would lead to improved mitochondrial activity afforded by pharmacological and nutritional agents. Of particular interest in this therapeutic strategy is thiamine, a water-soluble vitamin that plays an essential role in cellular energy metabolism. Critical illness associated with hypermetabolic states may predispose susceptible individuals to the development of thiamine deficiency, which is not usually identified by clinicians as a source of lactic acidosis. The protective effects of thiamine on mitochondrial function may justify supplementation in septic patients at risk of deficiency. Perspectives of supplementation with other micronutrients (ascorbic acid, tocopherol, selenium and zinc) and potential metabolic resuscitators [coenzyme Q10 (CoQ10), cytochrome oxidase (CytOx), L-carnitine, melatonin] to target sepsis-induced mitochondrial dysfunction are also emerging. Metabolic resuscitation may probably be a safe and effective strategy in the treatment of septic shock in the future. However, until then, preliminary investigations should be replicated in further researches for confirmation. Better identification of groups of patients presumed to benefit clinically by a certain intervention directed to "mitochondrial resuscitation" are expected to increase driven by genomics and metabolomics.
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spelling Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?Mitochondriasepsismultiple organ failureoxidative stressthiamineseleniumDespite the advances made in monitoring and treatment of sepsis and septic shock, many septic patients ultimately develop multiple organ dysfunction (MODS) and die, suggesting that other players are involved in the pathophysiology of this syndrome. Mitochondrial dysfunction occurs early in sepsis and has a central role in MODS development. MODS severity and recovery of mitochondrial function have been associated with survival. In recent clinical and experimental investigations, mitochondrion-target therapy for sepsis and septic shock has been suggested to reduce MODS severity and mortality. This intervention, which might be named "metabolic resuscitation", would lead to improved mitochondrial activity afforded by pharmacological and nutritional agents. Of particular interest in this therapeutic strategy is thiamine, a water-soluble vitamin that plays an essential role in cellular energy metabolism. Critical illness associated with hypermetabolic states may predispose susceptible individuals to the development of thiamine deficiency, which is not usually identified by clinicians as a source of lactic acidosis. The protective effects of thiamine on mitochondrial function may justify supplementation in septic patients at risk of deficiency. Perspectives of supplementation with other micronutrients (ascorbic acid, tocopherol, selenium and zinc) and potential metabolic resuscitators [coenzyme Q10 (CoQ10), cytochrome oxidase (CytOx), L-carnitine, melatonin] to target sepsis-induced mitochondrial dysfunction are also emerging. Metabolic resuscitation may probably be a safe and effective strategy in the treatment of septic shock in the future. However, until then, preliminary investigations should be replicated in further researches for confirmation. Better identification of groups of patients presumed to benefit clinically by a certain intervention directed to "mitochondrial resuscitation" are expected to increase driven by genomics and metabolomics.Univ Fed Sao Paulo, Dept Pediat, Discipline Nutr & Metab, Rua Loefgreen 1647, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Pediat, Pediat Intens Care Unit, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Pediat, Discipline Nutr & Metab, Rua Loefgreen 1647, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Pediat, Pediat Intens Care Unit, Sao Paulo, BrazilWeb of SciencePioneer Bioscience Publ Co2020-08-14T13:44:20Z2020-08-14T13:44:20Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionE552-E557application/pdfhttp://dx.doi.org/10.21037/jtd.2016.05.37Journal Of Thoracic Disease. Hong Kong, v. 8, n. 7, p. E552-E557, 2016.10.21037/jtd.2016.05.37WOS000385021800016.pdf2072-1439https://repositorio.unifesp.br/handle/11600/57604WOS:000385021800016ark:/48912/001300000b702porJournal Of Thoracic DiseaseHong Konginfo:eu-repo/semantics/openAccessLeite, Heitor Pons [UNIFESP]Peixoto de Lima, Lucio Flavio [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-01T09:04:19Zoai:repositorio.unifesp.br/:11600/57604Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:08:40.232473Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
title Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
spellingShingle Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
Leite, Heitor Pons [UNIFESP]
Mitochondria
sepsis
multiple organ failure
oxidative stress
thiamine
selenium
title_short Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
title_full Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
title_fullStr Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
title_full_unstemmed Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
title_sort Metabolic resuscitation in sepsis: a necessary step beyond the hemodynamic?
author Leite, Heitor Pons [UNIFESP]
author_facet Leite, Heitor Pons [UNIFESP]
Peixoto de Lima, Lucio Flavio [UNIFESP]
author_role author
author2 Peixoto de Lima, Lucio Flavio [UNIFESP]
author2_role author
dc.contributor.author.fl_str_mv Leite, Heitor Pons [UNIFESP]
Peixoto de Lima, Lucio Flavio [UNIFESP]
dc.subject.por.fl_str_mv Mitochondria
sepsis
multiple organ failure
oxidative stress
thiamine
selenium
topic Mitochondria
sepsis
multiple organ failure
oxidative stress
thiamine
selenium
description Despite the advances made in monitoring and treatment of sepsis and septic shock, many septic patients ultimately develop multiple organ dysfunction (MODS) and die, suggesting that other players are involved in the pathophysiology of this syndrome. Mitochondrial dysfunction occurs early in sepsis and has a central role in MODS development. MODS severity and recovery of mitochondrial function have been associated with survival. In recent clinical and experimental investigations, mitochondrion-target therapy for sepsis and septic shock has been suggested to reduce MODS severity and mortality. This intervention, which might be named "metabolic resuscitation", would lead to improved mitochondrial activity afforded by pharmacological and nutritional agents. Of particular interest in this therapeutic strategy is thiamine, a water-soluble vitamin that plays an essential role in cellular energy metabolism. Critical illness associated with hypermetabolic states may predispose susceptible individuals to the development of thiamine deficiency, which is not usually identified by clinicians as a source of lactic acidosis. The protective effects of thiamine on mitochondrial function may justify supplementation in septic patients at risk of deficiency. Perspectives of supplementation with other micronutrients (ascorbic acid, tocopherol, selenium and zinc) and potential metabolic resuscitators [coenzyme Q10 (CoQ10), cytochrome oxidase (CytOx), L-carnitine, melatonin] to target sepsis-induced mitochondrial dysfunction are also emerging. Metabolic resuscitation may probably be a safe and effective strategy in the treatment of septic shock in the future. However, until then, preliminary investigations should be replicated in further researches for confirmation. Better identification of groups of patients presumed to benefit clinically by a certain intervention directed to "mitochondrial resuscitation" are expected to increase driven by genomics and metabolomics.
publishDate 2016
dc.date.none.fl_str_mv 2016
2020-08-14T13:44:20Z
2020-08-14T13:44:20Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.21037/jtd.2016.05.37
Journal Of Thoracic Disease. Hong Kong, v. 8, n. 7, p. E552-E557, 2016.
10.21037/jtd.2016.05.37
WOS000385021800016.pdf
2072-1439
https://repositorio.unifesp.br/handle/11600/57604
WOS:000385021800016
dc.identifier.dark.fl_str_mv ark:/48912/001300000b702
url http://dx.doi.org/10.21037/jtd.2016.05.37
https://repositorio.unifesp.br/handle/11600/57604
identifier_str_mv Journal Of Thoracic Disease. Hong Kong, v. 8, n. 7, p. E552-E557, 2016.
10.21037/jtd.2016.05.37
WOS000385021800016.pdf
2072-1439
WOS:000385021800016
ark:/48912/001300000b702
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Journal Of Thoracic Disease
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv E552-E557
application/pdf
dc.coverage.none.fl_str_mv Hong Kong
dc.publisher.none.fl_str_mv Pioneer Bioscience Publ Co
publisher.none.fl_str_mv Pioneer Bioscience Publ Co
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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